A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498039



Internal ID275049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43324048..43324144hg38UCSC Ensembl
chr15:43616246..43616342hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702007
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498039
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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